物理性质
- 熔点139-143 °C
- 沸点589.3±60.0 °C at 760 mmHg
- 闪点310.2±32.9 °C
- 密度1.1±0.1 g/cm3
- pKa:9?+-.0.10(预测)
- PSA:50.94
- LogP:6.7779
- 折射率1.619
- 蒸汽压0.0±1.7 mmHg at 25°C
- 溶解性水: <0.04 Ppm At 20 °c, Insoluble
- 外观形态白色至类白色粉末
- 储存条件冰箱
- 产品应用本品是一个高分子量的紫外线吸收剂,对聚合物有杰出的光稳定作用,能广泛吸收300-400nm的紫外线和对可见光谱也有少量吸收.由于其能与多种物质相容和低的挥发性故很适合于高温和大表面积场合使用,如薄膜,纸张和纤维从而保护了制品中颜料受紫外线照射的破坏.可以广泛用于食品和药品的包装,允许和其它光稳定剂或抗氧剂一起使用. 主要用于聚碳酸酯,聚酯,聚缩醛,聚酰胺,聚苯硫醚,聚苯醚,芳香共聚物,热塑性聚氨基甲酸酯及聚氨基甲酸酯纤维.
- 性质描述熔点139-143°C,溶解性(20°C,每100ml溶剂能溶解的克数)水<0.01丙酮2甲苯20氯仿35二氯甲烷34环已烷5乙酸乙酯4正-已烷0.6甲醇<0.1乙醇0.3,质量标准:外观微黄粉末熔点137-141°C纯度≥99(HPLC)透光率460nm≥97500nm≥98挥发度≤0.3
欧盟法规
REACH注册ECHA物质ECHA物质C&L通报REACH预注册上下游产品
紫外光吸收剂 Uv-360 Methylene Bis-Benzotriazolyl Tetramethylbutylphenol 103597-45-1
3-(2H-苯并三唑-2-基)-5-(1,1-二甲基乙基)-4-羟基-苯丙酸甲酯 3-(3-(2H-Benzo[d][1,2,3]Triazol-2-yl)-5-(Tert-Butyl)-4-Hydroxyphenyl)Propionic Acid Methyl Ester 84268-33-7
2-(3'-Tert-Butyl-2'-Hydroxy-5'-(2-Octyloxycarbonylethyl)Phenyl)-Benzotriazole 84268-23-5
3-[3-叔-丁基-4-羟基-5-(5-氯-2H-苯并三唑-2-基)苯基]丙酸甲酯 2-[3'-Tert-Butyl-2'-Hydroxy-5'-(2-Methoxycarbonylethyl)Phenyl]-5-Chlorobenzotriazole 83044-91-1
2-(2H)-苯并三氮唑-2-基)-6-十二烷基-4-甲基苯酚 2-(2H-Benzotriazol-2-yl)-6-Dodecyl-4-Methylphenol 23328-53-2
3-[3-叔-丁基-4-羟基-5-(5-氯-2H-苯并三唑-2-基)苯基]丙酸辛酯 2-(3'-Tert-Butyl-2'-Hydroxy-5'-(2-Octyloxycarbonylethyl)Phenyl)-5-Chloro-Benzotriazole 83044-89-7
[5-羟基-4-(羟甲基)-6-甲基吡啶-3-基]甲基2-羟基苯酸酯 2-(3'-Tert-Butyl-5'-[2-(2-Ethyl-Hexyloxy)-Carbonylethyl]-2'-Hydroxyphenyl)-5-Chloro-Benzotriazole 83044-90-02-硝基苯重氮氯化物置于盐酸,甲醇,聚合甲醛,Sodium Hydroxide,锌体系中,用 乙醇,水,异丙醇,甲苯 作为反应溶剂,化学反应 3.0H,反应生成 紫外吸收剂 234
参考文献:一种紫外线吸收剂uv-234的制备方法
标题:一种紫外线吸收剂uv-234的制备方法
摘要:本发明提供了一种紫外线吸收剂uv‑234的制备方法,该方法包括由邻硝基氯苯经氨化,重氮化,偶合,一步还原,二步还原反应及后处理过程制备2‑[2'‑羟基‑3',5'‑双(α,α‑二甲基苄基)苯基]苯并三唑.本发明采用浓度为10%~25%的氨水将邻硝基氯苯氨化后再与亚硝酸盐经重氮化反应反应生成重氮盐,该重氮化反应无需在强酸介质下进行,且综合利用了本公司已有产品的副产品氨水,三废低排放,且所需成本低;中间体偶氮产物的还原闭环过程采用2步还原法,避免了强还原剂直接将偶氮双键还原成胺,减少杂质反应生成,不但提高了产品纯度,同时提高了产品收率.
海关参考信息
- 2902600000-乙苯
2902700000-异丙基苯
2907121100-间甲酚
2908199090-其他酚的卤化衍生物 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-2009318592-A1
优先权日:2005-10-11
标 题 :Process for the Synthesis of Amine Ethers
发明人:FREY MARKUS; BROENNIMANN VALERIE
权利人:CIBA GEIGY CORP
摘要:The present invention relates to novel processes for the preparation of a sterically hindered amine ether by reacting a corresponding sterically hindered amine oxide with a ketone or an aldehyde with at least one reactive H in the presence of a peroxydisulphate. Products obtained by this process may be hydrogenated. The compounds made by these processes are particularly effective in the stabilization of polymer compositions against harmful effects of light, oxygen and/or heat and as flame-retardants for polymers.
专利号:US-2007191516-A1
优先权日:2004-03-15
标题 :Process for the synthesis of amine ethers
发明人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
权利人:FREY MARKUS; RAST VALERIE; BRAIG ADALBERT; KRAMER ANDREAS
摘要:A process for the preparation of a sterically hindered amine ether which comprises reacting a corresponding sterically hindered aminoxide with a C 5 -C 18 alk-1-ene in the presence of an organic hydroperoxide and optionally hydrogenating the resulting product as well as the product mixtures obtained therewith and their use as stabilizers and flame retardants.
专利号:US-2023047214-A1
优先权日:2020-02-03
标题:Methods for microwave synthesis of degradable polymers for drug delivery
发明人:MURATOGLU ORHUN K; ORAL EBRU; GRINDY SCOTT
权利人:MASSACHUSETTS GEN HOSPITAL
摘要:Provided herein are methods of making degradable, additive-blended polymeric materials using microwave radiation and catalysts. The methods can include incorporation of therapeutic materials into the polymeric materials. There also are provided polymeric materials made by the methods and medical devices comprising the polymeric materials made by the methods.
专利号:US-7402675-B2
优先权日:2000-05-26
标题 :Process for the synthesis of amine ethers from secondary amino oxides
发明人:HAFNER ANDREAS; KIRNER HANS JUERG; SCHWARZENBACH FRANZ; VAN DER SCHAAF PAUL ADRIAAN; NESVADBA PETER
权利人:CIBA SC HOLDING AG
摘要:An amine ether of formula A n nwherein a is 1 or 2; and when a is 1, E is E′; when a is 2, E is L;n E′ is C 1 -C 36 alkyl; C 3 -C 18 alkenyl; C 2 -C 18 alkinyl; C 5 -C 18 cycloalkyl; C 5 -C 18 cycloalkenyl; a radical of a saturated or unsaturated aliphatic bicyclic or tricyclic hydrocarbon of 7 to 12 carbon atoms; C 2 -C 7 alkyl or C 3 -C 7 alkenyl substituted by halogen; C 7 -C 15 aralkyl or C 7 -C 15 aralkyl substituted by C 1 -C 4 alkyl or phenyl; or E′ is a radical of formula (VII) as explained in claim 1; T′ is tertiary C 4 -C 18 alkyl or phenyl, each of which are unsubstituted or substituted by halogen, OH, COOR 21 or C(O)—R 22 ; or T′ is C 5 -C 12 cycloalkyl; C 5 -C 12 cycloalkyl which is interrupted by at least one O or —NR 18 —; a polycyclic alkyl radical having 7-18 carbon atoms, or the same radical which is interrupted by at least one O or —NR 18 —; or T′ is —C(G 1 )(G 2 )-T″; or C 1 -C 18 alkyl or C 5 -C 12 cycloalkyl substituted by n n n n n n n n n n n n T″ is hydrogen, halogen, NO 2 , cyano, or is a monovalent organic radical comprising 1-50 carbon atoms; n or T″ and T′ together form a divalent organic linking group completing, together with the hindered amine nitrogen atom and the quaternary carbon atom substituted by G 1 and G 2 , an optionally substituted five- or six-membered ring structure; and all other residues are as defined in claim 1, n are obtained in good yield from the corresponding N-oxyl hindered amine precursor by reaction with a hydrocarbon E 1 -H or H-L-H in the presence of an organic hydroperoxide and a catalytic amount of copper or a copper compound. n n n n n The products of present process find utility as polymerization regulators and/or light stabilizers for organic material.
专利号:US-6417363-B1
优先权日:1997-12-04
标题 :Heterocyclyl ligand containing ruthenium and osmium catalysts
发明人:VAN DER SCHAAF PAUL ADRIAAN; MUEHLEBACH ANDREAS; HAFNER ANDREAS; KOLLY ROMAN
权利人:CIBA SC HOLDING AG
摘要:Penta- and hexa-coordinated, bridged ruthenium and osmium catalysts of the formulawherein Me is ruthenium or osmium; L1 and L2 are neutral ligands having electron donor properties;X is an anionic ligand; Y is oxygen or sulphur; A is a direct bond, C1-C4alkylene or C2-C4alkylidene;Z is a direct bond, oxygen, sulphur or the groupswherein R1 and R2 are hydrogen or hydrocarbon radicals; their preparation and their us in the synthesis of polymers, in the ring-closure metathesis of diolefins, in the cross metathesis of olefins and in the isomerisation of olefins are disclosed.
专利号:US-6077805-A
优先权日:1997-03-06
标题:Hexacoordinated ruthenium or osmium carbene catalysts
发明人:VAN DER SCHAAF PAUL ADRIAAN; HAFNER ANDREAS; MUEHLEBACH ANDREAS
权利人:CIBA SC HOLDING AG
摘要:Hexacoordinated ruthenium and osmium catalysts of the formulae in which M and M' independently of one another are ruthenium or osmium; X, X', Y and Y' independently of one another are anionic ligands, or X and Y and X' and Y' in each case together are bis-anionic ligands L1 and L1' independently of one another are tertiary phosphine; L2 and L3 independently of one another are a monodentate ligand, or L2 and L3 together are bidentate, neutral electron donor ligands; L4 is tetradentate, neutral electron donor ligand; L5 is a bidentate, neutral electron donor ligand; and T and T' indepedently of one another are H or organic substituents, are useful for the synthesis of custom-tailored polymers and for the ring-closing metathesis of olefins.